Svante Norgren

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome

René Santer, Sebastian Groth, Martina Kinner et al. · Human Genetics · 2001 · 170 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Increased β‐amyloid release and levels of amyloid precursor protein (APP) in fibroblast cell lines from family members with the Swedish Alzheimer's disease APP670/671 mutation

Janet Johnston, Richard F. Cowburn, Svante Norgren et al. · FEBS Letters · 1994 · 146 citations

Dental aberrations in children and adolescents with osteogenesis imperfecta

B. Malmgren, Svante Norgren · Acta Odontologica Scandinavica · 2002 · 131 citations · Full text

Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type�II

B. Malmgren, S. Lindskog, Aziz Elgadi et al. · Human Genetics · 2004 · 104 citations

Dental Morphology, Developmental Biology, Dentinogenesis Imperfecta Type�ii +7

Transthyretin constitutes a functional component in pancreatic β-cell stimulus-secretion coupling

Essam Refai, Nancy Dekki, Shao-Nian Yang et al. · Proceedings of the National Academy of Sciences · 2005 · 101 citations · Full text